Assessment of the Safety and Feasibility of a High-intensity Interval Training Program in Adult CF Patients: a Randomized Bicentric Pilot Study

Status: Completed
Location: See all (2) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study compare an usual training program (in continuous endurance) with an ITHI program over a period of 3 weeks, in France. The aim is to evaluate the safety and feasibility of this type of program in CF adults, and also more specifically, in subgroups: patients divided according to the severity of their FEV1 ; patients treated with modulating CFTR canal therapy ; diabetic patients on insulin ; undernourished patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• men and women aged over 18 years of age on the date of informed consent

• diagnosed CF patients

• not transplanted and not on the transplant waiting list

• able to participate in the proposed training programs (especially without cardiac contraindication)

• able to understand and respect the protocol and its requirement

• who signed the consent prior to any other procedure protocol

Locations
Other Locations
France
CF Center of Giens - Hospices Civils de Lyon Hôpital Renée Sabran
Giens
CF Center - Fondation Ildys Site de Perharidy
Roscoff
Time Frame
Start Date: 2021-09-01
Completion Date: 2023-09-13
Participants
Target number of participants: 62
Treatments
No_intervention: Control group
Patients benefiting from the usual re-training sessions
Experimental: ITHI Group
Patients benefiting from ITHI re-training sessions
Authors
Jean Le Bihan, Laurent Mely, Sophie Ramel
Related Therapeutic Areas
Sponsors
Leads: Fondation Ildys
Collaborators: Lille Catholic University

This content was sourced from clinicaltrials.gov